A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560860



Internal ID20933931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:109914371..110480797hg38UCSC Ensembl
chr7:109554428..110120854hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38566427
hg19566427
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273640
Samples
Known GenesEIF3IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560860
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer